Gopalkrishnan Saumya, Nicoloff Herve, Ades Sarah E
Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA, 16802, USA.
Mol Microbiol. 2014 Aug;93(3):479-93. doi: 10.1111/mmi.12674. Epub 2014 Jul 10.
The E. coli alternative sigma factor, σ(E) , transcribes genes required to maintain the cell envelope and is activated by conditions that destabilize the envelope. σ(E) is also activated during entry into stationary phase in the absence of envelope stress by the alarmone (p)ppGpp. (p)ppGpp controls a large regulatory network, reducing expression of σ(70) -dependent genes required for rapid growth and activating σ(70) -dependent and alternative sigma factor-dependent genes required for stress survival. The DksA protein often potentiates the effects of (p)ppGpp. Here we examine regulation of σ(E) by (p)ppGpp and DksA following starvation for nutrients. We find that (p)ppGpp is required for increased σ(E) activity under all conditions tested, but the requirement for DksA varies. DksA is required during amino acid starvation, but is dispensable during phosphate starvation. In contrast, regulation of σ(S) is (p)ppGpp- and DksA-dependent under all conditions tested, while negative regulation of σ(70) is DksA- but not (p)ppGpp-dependent during phosphate starvation, yet requires both factors during amino acid starvation. These findings suggest that the mechanism of transcriptional regulation by (p)ppGpp and/or DksA cannot yet be explained by a unifying model and is specific to individual promoters, individual holoenzymes, and specific starvation conditions.
大肠杆菌的替代西格玛因子σ(E)转录维持细胞包膜所需的基因,并在包膜不稳定的条件下被激活。在没有包膜应激的情况下,进入稳定期时,警报素(p)ppGpp也会激活σ(E)。(p)ppGpp控制着一个庞大的调控网络,降低快速生长所需的依赖σ(70)的基因的表达,并激活应激存活所需的依赖σ(70)和替代西格玛因子的基因。DksA蛋白通常会增强(p)ppGpp的作用。在这里,我们研究了营养物质饥饿后(p)ppGpp和DksA对σ(E)的调控。我们发现,在所有测试条件下,增加σ(E)活性都需要(p)ppGpp,但对DksA的需求各不相同。在氨基酸饥饿期间需要DksA,但在磷酸盐饥饿期间则不需要。相比之下,在所有测试条件下,σ(S)的调控都依赖于(p)ppGpp和DksA,而在磷酸盐饥饿期间,σ(70)的负调控依赖于DksA而不依赖于(p)ppGpp,但在氨基酸饥饿期间则需要这两种因子。这些发现表明,(p)ppGpp和/或DksA的转录调控机制尚不能用一个统一的模型来解释,并且特定于个别启动子、个别全酶和特定的饥饿条件。